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FDA 510(k)

PBN DRAINAGE CATHETER GUIDEWIRES

K-Number: K991097 · 1999-04-23

ApplicantMedical Device Technologies, Inc.
Decision Date1999-04-23
Product CodeKNY
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PBN DRAINAGE CATHETER GUIDEWIRES is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Technologies, Inc.. It received FDA 510(k) clearance on 1999-04-23 under 510(k) number K991097. The device is classified under product code KNY. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PBN DRAINAGE CATHETER GUIDEWIRES?

PBN DRAINAGE CATHETER GUIDEWIRES is a medical device that received FDA 510(k) clearance on 1999-04-23. The listed applicant is Medical Device Technologies, Inc.. The 510(k) number is K991097.

When did PBN DRAINAGE CATHETER GUIDEWIRES receive FDA 510(k) clearance?

PBN DRAINAGE CATHETER GUIDEWIRES received FDA 510(k) clearance on 1999-04-23, under 510(k) number K991097.

Who is the listed applicant for PBN DRAINAGE CATHETER GUIDEWIRES?

The FDA 510(k) record lists Medical Device Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PBN DRAINAGE CATHETER GUIDEWIRES?

The FDA product code for PBN DRAINAGE CATHETER GUIDEWIRES is KNY.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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